Computerized System Validation (CSV) Manager
This role manages the validation of computerized systems within the pharmaceutical sector. It offers a flexible schedule, hybrid work, and a flexible benefits plan.
The English-language job board for Spain
87,000+ live jobsHybrid in Barcelona·Added 2 months ago (last checked 15 Oct)
15 open roles
The ad doesn’t mention sponsorship
Not a refusal, but not a yes. Worth asking in your first message.
This job advert was originally written in Spanish.
REQUIREMENTS 🤹:
• 1-2 years of experience performing the tasks described.
• Good command of office software at an advanced level: Microsoft Office.
• 1+ year of experience in Periodic Reviews and Execution of Validations.
• Knowledge of GxP regulations in the pharmaceutical sector.
• Knowledge of 21 CFR Part 11 and EU GMP Annex 11 regulations.
• Knowledge of GAMP 5.
• Valid driver's license and own vehicle.
• University studies with a postgraduate degree or Master's (Chemical Engineering, Industrial Engineering, Chemistry, Biology, Biotechnology).
• English proficiency (B2+/C1).
Negotiable salary.
Permanent contract.
Restaurant tickets for the days you go to the office.
Flexible compensation plan (tax-free), we provide: private health insurance, public transport pass, and childcare voucher.
Discounts for access to fitness centers (Urban Sports Club)
Learning and development (training catalog)
Referral program.
An organization with highly professional people to grow with.
Our goal is your well-being in every sense!
We are looking for a passionate "Junior Validation Technician" to join our incredible LifeScience team. As part of this exciting role, you will be involved in a variety of interesting projects.
Generation of validation documentation (Validation Plan, Risk Analysis, Qualification Protocols: IQ, OQ, PQ, reports).
Support in the execution of qualification protocols.
Maintenance of validation status: performance of Periodic Review.
Communication with the work team (project status, detected incidents, etc.).
Continuous training.
SCHEDULE 🕘:
Monday to Friday (From 8-9 am to 5-6 pm - flexible).
Hybrid model: 2 days in the office and 3 remote.
Location: Barcelona.
Ambit Iberia is a specialized consultancy providing IT and engineering services to the pharmaceutical and life sciences sectors, with a strong focus on regulated environments. The company supports clients with digital transformation, data integrity, and compliance-driven projects, offering services such as system validation, MES engineering, cybersecurity, and cloud-based software development. Operating primarily in Spain and Portugal, Ambit Iberia positions itself as a niche partner for pharma companies seeking technical expertise in highly regulated settings.
With its main office in Barcelona, Ambit Iberia serves as the Spanish arm of a broader international group, delivering projects across Europe. The company's work culture emphasizes technical excellence and regulatory compliance, making it an attractive option for international professionals with backgrounds in pharma IT, validation, and engineering. Many roles are offered as fully remote or hybrid, allowing flexibility for candidates based in Spain or Portugal, and the company actively seeks talent with experience in GxP environments and modern cloud technologies.